Human Genome Epidemiology Literature Finder
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Query Trace: Hypokalemia and SRY[original query] |
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Clinical and Genetic Characteristics of 17 ?-Hydroxylase/17, 20-Lyase Deficiency: c.985_987delTACinsAA Mutation of CYP17A1 Prevalent in the Chinese Han Population. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 Dec . Xia Junke, Liu Furong, Wu Jing, Xia Yanjie, Zhao Zhenhua, Zhao Yongjiang, Ren Huayan, Kong Xiangdo |
- Page last reviewed:Feb 1, 2024
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